| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:36574397-36574601 | Rare:72 | ||||
| chr20:36746062-36746245 | Common:2; Rare:70 | ||||
| chr20:36951627-36951914 | Common:1; Rare:89; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:37095953-37096269 | Common:1; Rare:101 | ||||
| chr20:37178865-37179195 | Rare:96 | ||||
| chr20:37289605-37289669 | Common:1; Rare:20 | ||||
| chr20:37527820-37528175 | Common:4; Rare:123 | ||||
| chr20:38033402-38033775 | Common:2; Rare:109 | ||||
| chr20:38805605-38805723 | Common:2; Rare:28 | ||||
| chr20:38926118-38926433 | Common:4; Rare:107 | ||||
| chr20:38962106-38962388 | Common:2; Rare:117 | ||||
| chr20:41028593-41028878 | Rare:109 | ||||
| chr20:43457805-43458052 | Rare:127 | ||||
| chr20:43458253-43458413 | Common:2; Rare:65 | ||||
| chr20:43590650-43590983 | Rare:73 |